JP2013534144A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2013534144A5 JP2013534144A5 JP2013524893A JP2013524893A JP2013534144A5 JP 2013534144 A5 JP2013534144 A5 JP 2013534144A5 JP 2013524893 A JP2013524893 A JP 2013524893A JP 2013524893 A JP2013524893 A JP 2013524893A JP 2013534144 A5 JP2013534144 A5 JP 2013534144A5
- Authority
- JP
- Japan
- Prior art keywords
- composition
- temperature
- bioorganic
- surfactant
- host cell
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000203 mixture Substances 0.000 claims description 34
- 239000004094 surface-active agent Substances 0.000 claims description 7
- 239000000839 emulsion Substances 0.000 claims description 2
- 238000000746 purification Methods 0.000 claims description 2
- -1 polyoxyethylene Polymers 0.000 claims 7
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims 6
- 241000195649 Chlorella <Chlorellales> Species 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 239000007764 o/w emulsion Substances 0.000 claims 4
- JSNRRGGBADWTMC-UHFFFAOYSA-N (6E)-7,11-dimethyl-3-methylene-1,6,10-dodecatriene Chemical compound CC(C)=CCCC(C)=CCCC(=C)C=C JSNRRGGBADWTMC-UHFFFAOYSA-N 0.000 claims 2
- JSNRRGGBADWTMC-QINSGFPZSA-N (E)-beta-Farnesene Natural products CC(C)=CCC\C(C)=C/CCC(=C)C=C JSNRRGGBADWTMC-QINSGFPZSA-N 0.000 claims 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims 2
- 229930009668 farnesenes Natural products 0.000 claims 2
- 229920000570 polyether Polymers 0.000 claims 2
- 229920005862 polyol Polymers 0.000 claims 2
- 150000003077 polyols Chemical class 0.000 claims 2
- 150000003505 terpenes Chemical class 0.000 claims 2
- 241000193830 Bacillus <bacterium> Species 0.000 claims 1
- 241000894006 Bacteria Species 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 241000195493 Cryptophyta Species 0.000 claims 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N Diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims 1
- 241000588722 Escherichia Species 0.000 claims 1
- 241000233866 Fungi Species 0.000 claims 1
- 229940039696 Lactobacillus Drugs 0.000 claims 1
- 241000186660 Lactobacillus Species 0.000 claims 1
- 241000195659 Neodesmus pupukensis Species 0.000 claims 1
- 241000235648 Pichia Species 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 241000235070 Saccharomyces Species 0.000 claims 1
- 235000003534 Saccharomyces carlsbergensis Nutrition 0.000 claims 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims 1
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 claims 1
- 229940081969 Saccharomyces cerevisiae Drugs 0.000 claims 1
- 241000235013 Yarrowia Species 0.000 claims 1
- 150000005215 alkyl ethers Chemical class 0.000 claims 1
- 125000000891 alpha-farnesene group Chemical group 0.000 claims 1
- 229930002150 alpha-farnesenes Natural products 0.000 claims 1
- 230000003078 antioxidant Effects 0.000 claims 1
- 239000003963 antioxidant agent Substances 0.000 claims 1
- 229930004079 beta-farnesenes Natural products 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- 238000007701 flash-distillation Methods 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000002736 nonionic surfactant Substances 0.000 claims 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000002530 phenolic antioxidant Substances 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 238000000926 separation method Methods 0.000 claims 1
- 241000894007 species Species 0.000 claims 1
- 239000007762 w/o emulsion Substances 0.000 claims 1
- 239000012071 phase Substances 0.000 description 5
- 239000002738 chelating agent Substances 0.000 description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N edta Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- DIWZKTYQKVKILN-VKHMYHEASA-N (2S)-2-(dicarboxymethylamino)pentanedioic acid Chemical compound OC(=O)CC[C@@H](C(O)=O)NC(C(O)=O)C(O)=O DIWZKTYQKVKILN-VKHMYHEASA-N 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Vitamin C Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- YIKPWSKEXRZQIY-UHFFFAOYSA-N butanedioic acid;ethane-1,2-diamine Chemical compound NCCN.OC(=O)CCC(O)=O.OC(=O)CCC(O)=O YIKPWSKEXRZQIY-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N fumaric acid Chemical compound OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
Images
Description
油相の水相に対する比は、組成物又はエマルションのPITに影響を与え得る。一般に、PITは、油相の水相に対する比の上昇と共に上昇する。さらに、界面活性剤の濃度が低ければ低いほど、PITの上昇率が高くなる。一部の実施態様では、油相の水相に対する比は、約1:100〜約100:1、約1:50〜約50:1、約1:20〜約20:1、約1:10〜約10:1、約1:8〜約8:1、約1:6〜約6:1、約1:5〜約5:1、約1:4〜約4:1、約1:3〜約3:1、又は約1:2〜約2:1である。
The ratio of oil phase to water phase can affect the PIT of the composition or emulsion. In general, PIT increases with increasing ratio of oil phase to water phase. Furthermore, the lower the surfactant concentration, the higher the rate of increase in PIT. In some embodiments, the ratio of oil phase to aqueous phase is about 1: 100 to about 100: 1, about 1:50 to about 50: 1 , about 1:20 to about 20: 1, about 1:10. To about 10: 1, about 1: 8 to about 8: 1, about 1: 6 to about 6: 1, about 1: 5 to about 5: 1, about 1: 4 to about 4: 1, about 1: 3 To about 3: 1, or from about 1: 2 to about 2: 1.
別の例では、精製組成物を、キレート剤の添加により仕上げ精製して該組成物中の金属の量を減少させることができる。特定の実施態様では、精製工程は、キレート剤の添加によって粗生物有機組成物中に存在する金属を除去する工程も含む。任意の適切なキレート剤を使用することができる。適切なキレート剤の実例として、アスコルビン酸、クエン酸、マレイン酸、シュウ酸、コハク酸、ジカルボキシメチルグルタミン酸、エチレンジアミンジコハク酸(EDDS)、及びエチレンジアミンテトラ酢酸(EDTA)などが挙げられる。
In another example, the purified composition can be final purified by the addition of a chelating agent to reduce the amount of metal in the composition. In certain embodiments, the purification step also includes removing metals present in the crude bioorganic composition by the addition of a chelating agent. Any suitable chelating agent can be used. Illustrative of suitable chelating agents, ascorbic acid, citric acid, maleic acid, oxalic acid, succinic acid, di-carboxymethyl glutamic acid, ethylenediamine disuccinic acid (EDDS), and the like ethylenediaminetetraacetic acid (EDTA).
Claims (15)
(b)該水中油型エマルションの温度を、該相反転温度よりも少なくとも約1℃高い温度まで上昇させ、それによって、該水中油型エマルションを油中水型エマルションに変換する工程;及び
(c)該組成物の液液分離を行って粗生物有機組成物を提供する工程を含む、方法。 (a) providing a composition comprising a surfactant, a host cell, an aqueous medium, a bio-organic compound produced by the host cell, and an oil-in-water emulsion formed therefrom, comprising the step of: Wherein the solubility of the surfactant decreases with increasing temperature, and the temperature of the composition is at least about 1 ° C. lower than the phase inversion temperature of the composition;
(b) raising the temperature of the oil-in-water emulsion to a temperature at least about 1 ° C. above the phase inversion temperature, thereby converting the oil-in-water emulsion to a water-in-oil emulsion; and
(c) A method comprising liquid-liquid separation of the composition to provide a crude bioorganic composition.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US37387610P | 2010-08-16 | 2010-08-16 | |
US61/373,876 | 2010-08-16 | ||
PCT/US2011/047616 WO2012024186A1 (en) | 2010-08-16 | 2011-08-12 | Method for purifying bio-organic compounds from fermentation broth containing surfactants by temperature-induced phase inversion |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013534144A JP2013534144A (en) | 2013-09-02 |
JP2013534144A5 true JP2013534144A5 (en) | 2014-04-17 |
Family
ID=44515045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013524893A Pending JP2013534144A (en) | 2010-08-16 | 2011-08-12 | Method for purifying bioorganic compounds from fermentation broths containing surfactants by temperature-induced phase inversion |
Country Status (11)
Country | Link |
---|---|
US (1) | US20120040396A1 (en) |
EP (1) | EP2606018A1 (en) |
JP (1) | JP2013534144A (en) |
KR (1) | KR20130108064A (en) |
CN (1) | CN103052612A (en) |
AU (1) | AU2011292231B2 (en) |
BR (1) | BR112012027462A2 (en) |
CA (1) | CA2796438A1 (en) |
MX (1) | MX2012012705A (en) |
WO (1) | WO2012024186A1 (en) |
ZA (1) | ZA201207717B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20150087039A1 (en) * | 2012-03-07 | 2015-03-26 | Abengoa Bioenergy New Technologies, Llc | Methods for enhancing the recovery of oil during biofuel production |
PT3110930T (en) | 2014-02-28 | 2020-06-16 | Delft Advanced Biofuels B V | Process for the recovery of lipids or hydrocarbons |
EP3665292B1 (en) | 2017-08-07 | 2024-03-06 | Total Raffinage Chimie | Process for recovering isoprenoids produced by microorganisms |
JP7504031B2 (en) * | 2018-06-29 | 2024-06-21 | アミリス, インコーポレイテッド | Method for recovering water insoluble isoprenoid compounds from microbial biomass - Patents.com |
EP3766982A1 (en) | 2019-07-18 | 2021-01-20 | Delft Advanced Biofuels B.V. | Integrated system for biocatalytically producing and recovering an organic substance |
WO2024147836A1 (en) | 2023-01-03 | 2024-07-11 | Amyris, Inc. | Host cells capable of producing sequiterpenoids and methods of use thereof |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2427326A (en) * | 1945-02-13 | 1947-09-09 | Socony Vacuum Oil Co Inc | Treatment of mineral oil emulsions |
US2782244A (en) * | 1952-01-24 | 1957-02-19 | Phillips Petroleum Co | Isomerizing hydrocarbons with the catalyst in the continuous phase inverting the phases and separating the catalyst employing phase inversion |
US4725287A (en) * | 1986-11-24 | 1988-02-16 | Canadian Occidental Petroleum, Ltd. | Preparation of stable crude oil transport emulsions |
US5730905A (en) * | 1994-06-21 | 1998-03-24 | Betzdearborn Inc. | Method of resolving oil and water emulsions |
US6431370B1 (en) * | 1995-01-27 | 2002-08-13 | Genencor International, Inc. | Direct enzyme agglomeration process |
WO2000058342A1 (en) * | 1999-03-25 | 2000-10-05 | Valtion Teknillinen Tutkimuskeskus | Process for partitioning of proteins |
DE10035930A1 (en) * | 2000-07-21 | 2002-01-31 | Clariant Gmbh | fine emulsions |
US7179311B2 (en) * | 2003-01-31 | 2007-02-20 | Chevron U.S.A. Inc. | Stable olefinic, low sulfur diesel fuels |
CN1246451C (en) * | 2003-08-07 | 2006-03-22 | 上海来益生物药物研究开发中心有限责任公司 | Application of cloud point system in biotransformation |
MY163029A (en) | 2006-05-26 | 2017-07-31 | Amyris Inc | Apparatus for making bio-organic compounds |
DK2024504T4 (en) | 2006-05-26 | 2023-02-27 | Amyris Inc | Production of isoprenoids |
BRPI0713105B8 (en) * | 2006-05-26 | 2021-05-25 | Amyris Biotechnologies Inc | method for producing an isoprenoid |
US7846222B2 (en) | 2006-10-10 | 2010-12-07 | Amyris Biotechnologies, Inc. | Fuel compositions comprising farnesane and farnesane derivatives and method of making and using same |
WO2008140492A2 (en) | 2006-11-21 | 2008-11-20 | Amyris Biotechnologies, Inc. | Jet fuel compositions and methods of making and using same |
BRPI0718973A2 (en) | 2006-11-21 | 2014-02-04 | Amyris Biotechnologies Inc | FUEL COMPOSITION, METHODS FOR PREPARING FUEL COMPOSITION, AND FOR DRIVING AN ENGINE, AND VEHICLE |
CN101260137B (en) * | 2007-03-07 | 2010-12-08 | 中国科学院过程工程研究所 | Method for purifying and refining glycyrrhetic acid from liquorice by microwave auxiliary cloud point extraction |
US8110093B2 (en) | 2007-03-14 | 2012-02-07 | Ls9, Inc. | Process for producing low molecular weight hydrocarbons from renewable resources |
WO2008151149A2 (en) | 2007-06-01 | 2008-12-11 | Solazyme, Inc. | Production of oil in microorganisms |
KR101307686B1 (en) | 2007-07-20 | 2013-09-12 | 아미리스 인코퍼레이티드 | Fuel compositions comprising tetramethylcyclohexane |
CA2723163A1 (en) | 2008-05-02 | 2009-11-05 | Amyris Biotechnologies, Inc. | Fuel compositions comprising an amorphane or a stereoisomer thereof and methods of making and using same |
US7655739B1 (en) | 2009-06-26 | 2010-02-02 | Amyris Biotechnologies, Inc. | Adhesive compositions comprising a polyfarnesene |
US7589243B1 (en) | 2008-09-17 | 2009-09-15 | Amyris Biotechnologies, Inc. | Jet fuel compositions |
US7592295B1 (en) | 2008-10-10 | 2009-09-22 | Amyris Biotechnologies, Inc. | Farnesene dimers and/or farnesane dimers and compositions thereof |
-
2011
- 2011-08-05 US US13/198,711 patent/US20120040396A1/en not_active Abandoned
- 2011-08-12 BR BR112012027462A patent/BR112012027462A2/en not_active IP Right Cessation
- 2011-08-12 CN CN2011800374729A patent/CN103052612A/en active Pending
- 2011-08-12 CA CA2796438A patent/CA2796438A1/en not_active Abandoned
- 2011-08-12 MX MX2012012705A patent/MX2012012705A/en not_active Application Discontinuation
- 2011-08-12 WO PCT/US2011/047616 patent/WO2012024186A1/en active Application Filing
- 2011-08-12 KR KR1020127028294A patent/KR20130108064A/en not_active Application Discontinuation
- 2011-08-12 AU AU2011292231A patent/AU2011292231B2/en not_active Ceased
- 2011-08-12 JP JP2013524893A patent/JP2013534144A/en active Pending
- 2011-08-12 ZA ZA201207717A patent/ZA201207717B/en unknown
- 2011-08-12 EP EP11749297.5A patent/EP2606018A1/en not_active Withdrawn
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2013534144A5 (en) | ||
Wang et al. | Recovery of rare earth elements with ionic liquids | |
RU2012115519A (en) | APPLICATION OF ALK (EN) ILOLIGOGLYCOSIDES IN PROCESSES WITH HIGHER OIL REMOVAL | |
CN101759230B (en) | Method for fractionating, extracting and separating zirconium and hafnium | |
CN102826728A (en) | Cleaning agent applied to treatment of oily sludge by hot washing method and preparation method thereof | |
CN103459561A (en) | Synergistic H2S/mercaptan scavengers using glyoxal | |
WO2015109901A1 (en) | Extracting agent for treating coking wastewater | |
MY175750A (en) | A water-soluble metal working oil composition, a method of grinding a metal and a ground product | |
CA2798180A1 (en) | Non-aqueous taxane pro-emulsion formulations and methods of making and using the same | |
CN104099621A (en) | Weakly alkaline environment-friendly aluminum product surface degreasing agent and preparation method thereof | |
CN103469225A (en) | Cleaning agent for fast deoiling and descaling and method for cleaning workpiece by using same | |
NZ702064A (en) | Oxygen scavenging compositions | |
CN106883833A (en) | For the oil displacement system of ultrahigh-temperature high salt high rigidity oil reservoir | |
CN103320108B (en) | Wax-removing agent and preparation method thereof | |
CN103409759B (en) | A kind of acidic detergent for metal | |
JP2014532123A5 (en) | ||
CN102925685A (en) | Compound solvent for extraction separation of tungsten and molybdenum and using method thereof | |
CN101712885B (en) | Dehydration demulsifier for mud-containing produced liquid | |
JP2013226514A (en) | Method for treating dewatered sludge | |
CN106414676A (en) | Oxidation-stabilized biodiesel | |
RU2012118607A (en) | CLEANING COMPOSITION FOR SOLID SURFACES | |
JP2007275830A (en) | Method for recovering nitric acid from acetic acid-nitric acid-phosphoric acid type mixed waste liquid | |
RU2015136901A (en) | Cleaning compositions containing low HLB 2-propylheptyl alcohol alkoxylates and alkyl polyglycosides | |
CN103980933B (en) | A kind of for condensate oil fast dewatering emulsion splitter and preparation method after acid fracturing | |
CN104593120A (en) | Demulsifier |